GVI phospholipase A2 role in the stimulatory effect of sphingosine-1-phosphate on TRPC5 cationic channels-Reference-Cited by-同舟云学术

GVI phospholipase A2 role in the stimulatory effect of sphingosine-1-phosphate on TRPC5 cationic channels

Published:2011-10 Issue:4 Volume:50 Page:343-350
ISSN:0143-4160
Container-title:Cell Calcium
language:en
Short-container-title:Cell Calcium

Author:

AL-Shawaf Eman,Tumova Sarka,Naylor Jacqueline,Majeed Yasser,Li Jing,Beech David J.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Physiology

Reference56 articles.

1. TRPC4 and TRPC5: receptor-operated Ca2+-permeable nonselective cation channels;Plant;Cell Calcium,2003

2. Properties and therapeutic potential of transient receptor potential channels with putative roles in adversity: focus on TRPC5, TRPM2 and TRPA1;Jiang;Curr. Drug Targets,2011

3. Transient receptor potential cation channels in disease;Nilius;Physiol. Rev.,2007

4. Physiology and pathophysiology of canonical transient receptor potential channels;Abramowitz;Faseb J.,2009

5. TRPC5 is a regulator of hippocampal neurite length and growth cone morphology;Greka;Nat. Neurosci.,2003

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